Direkt zum Inhalt
Merck

Ruthenium-catalyzed transformation of aryl and alkenyl triflates to halides.

Journal of the American Chemical Society (2012-08-25)
Yusuke Imazaki, Eiji Shirakawa, Ryota Ueno, Tamio Hayashi
ZUSAMMENFASSUNG

Aryl triflates were transformed to aryl bromides/iodides simply by treating them with LiBr/NaI and [Cp*Ru(MeCN)(3)]OTf. The ruthenium complex also catalyzed the transformation of alkenyl sulfonates and phosphates to alkenyl halides under mild conditions. Aryl and alkenyl triflates undergo oxidative addition to a ruthenium(II) complex to form η(1)-arylruthenium and 1-ruthenacyclopropene intermediates, respectively, which are transformed to the corresponding halides.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Zinktrifluormethansulfonat, 98%
Sigma-Aldrich
Trifluormethansulfonsäure, ReagentPlus®, ≥99%
Sigma-Aldrich
Silbertrifluormethansulfonat, ≥99%
Sigma-Aldrich
Trifluormethansulfonsäure, reagent grade, 98%
Sigma-Aldrich
Aluminiumtrifluormethansulfonat, 99.9% trace metals basis
Sigma-Aldrich
Lithiumtrifluormethansulfonat, 99.995% trace metals basis
Sigma-Aldrich
Silbertrifluormethansulfonat, ≥99.95% trace metals basis
Sigma-Aldrich
Lanthan(III)-trifluormethansulfonat, 99.999% trace metals basis
Sigma-Aldrich
Lithiumtrifluormethansulfonat, 96%
Sigma-Aldrich
Silbertrifluormethansulfonat, purum, ≥98.0% (Ag)
Sigma-Aldrich
Bariumtrifluormethansulfonat, 98%